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MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1

BACKGROUND: Colorectal cancer (CRC), a common malignancy worldwide, and microRNAs (miRs) have been suggested to play roles in the disease. MiR-566 expression has been shown to be reduced in CRC, but its functions and mechanisms are still unclear. METHODS: Cell viability was assessed by using the Cel...

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Autores principales: Zhang, Ying, Zhang, Siqi, Yin, Jian, Xu, Ruisi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907181/
https://www.ncbi.nlm.nih.gov/pubmed/31866763
http://dx.doi.org/10.1186/s12935-019-1053-1
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author Zhang, Ying
Zhang, Siqi
Yin, Jian
Xu, Ruisi
author_facet Zhang, Ying
Zhang, Siqi
Yin, Jian
Xu, Ruisi
author_sort Zhang, Ying
collection PubMed
description BACKGROUND: Colorectal cancer (CRC), a common malignancy worldwide, and microRNAs (miRs) have been suggested to play roles in the disease. MiR-566 expression has been shown to be reduced in CRC, but its functions and mechanisms are still unclear. METHODS: Cell viability was assessed by using the CellTiter 96 AQueous One Solution Cell Proliferation kit. Cell proliferation was measured with MTT assay. Cell metastasis were measured by transwell assay. Luciferase reporter assays was used to confirm the target of MiR-566. PSKH1 expression was measured by RT-PCR and western blot. RESULTS: In the present study, we first observed that miR-566 was expressed in several CRC cell lines (SW480, SW620, LoVo, HT29 and Caco-2) at low levels compared to control colon epithelial cell lines (FHC). Further study showed that miR-566 overexpression suppressed cell survival and impeded cell proliferation, whereas inhibition of its expression enhanced cell survival and proliferation. Transwell assays showed that cell invasion and migration were reduced in cells overexpressing miR-566 and increased in those with inhibition of miR-566. Further analysis confirmed that PSKH1 is a target of miR-566. MiR-566 overexpression significantly inhibited PSKH1 expression and reintroduction of PSKH1 partially reversed the effects of miR-566 on CRC cell growth and metastasis in SW480 and Caco-2 cells. CONCLUSIONS: Taken together, the data show that CRC cell growth and metastasis can be significantly suppressed by miR-566 through targeting PSKH1.
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spelling pubmed-69071812019-12-20 MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1 Zhang, Ying Zhang, Siqi Yin, Jian Xu, Ruisi Cancer Cell Int Primary Research BACKGROUND: Colorectal cancer (CRC), a common malignancy worldwide, and microRNAs (miRs) have been suggested to play roles in the disease. MiR-566 expression has been shown to be reduced in CRC, but its functions and mechanisms are still unclear. METHODS: Cell viability was assessed by using the CellTiter 96 AQueous One Solution Cell Proliferation kit. Cell proliferation was measured with MTT assay. Cell metastasis were measured by transwell assay. Luciferase reporter assays was used to confirm the target of MiR-566. PSKH1 expression was measured by RT-PCR and western blot. RESULTS: In the present study, we first observed that miR-566 was expressed in several CRC cell lines (SW480, SW620, LoVo, HT29 and Caco-2) at low levels compared to control colon epithelial cell lines (FHC). Further study showed that miR-566 overexpression suppressed cell survival and impeded cell proliferation, whereas inhibition of its expression enhanced cell survival and proliferation. Transwell assays showed that cell invasion and migration were reduced in cells overexpressing miR-566 and increased in those with inhibition of miR-566. Further analysis confirmed that PSKH1 is a target of miR-566. MiR-566 overexpression significantly inhibited PSKH1 expression and reintroduction of PSKH1 partially reversed the effects of miR-566 on CRC cell growth and metastasis in SW480 and Caco-2 cells. CONCLUSIONS: Taken together, the data show that CRC cell growth and metastasis can be significantly suppressed by miR-566 through targeting PSKH1. BioMed Central 2019-12-11 /pmc/articles/PMC6907181/ /pubmed/31866763 http://dx.doi.org/10.1186/s12935-019-1053-1 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Primary Research
Zhang, Ying
Zhang, Siqi
Yin, Jian
Xu, Ruisi
MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1
title MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1
title_full MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1
title_fullStr MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1
title_full_unstemmed MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1
title_short MiR-566 mediates cell migration and invasion in colon cancer cells by direct targeting of PSKH1
title_sort mir-566 mediates cell migration and invasion in colon cancer cells by direct targeting of pskh1
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907181/
https://www.ncbi.nlm.nih.gov/pubmed/31866763
http://dx.doi.org/10.1186/s12935-019-1053-1
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